A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880570



Internal ID22655540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97173261..97173316hg38UCSC Ensembl
chr1:97638817..97638872hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404472
Samples
Known GenesDPYD, DPYD-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880570
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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